Joseph A. Sparano

Albert Einstein College of Medicine
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Articles (17)

Year:

2025

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2025

Year:

2025

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2025

Year:

2024

Year:

2023

Purpose: Endocrine-based therapy is the initial primary treatment option for hormone receptor–positive and human epidermal growth factor receptor 2-negative (HR+/HER2−) metastatic breast cancer (mBC). However, patients eventually experience disease progression due to resistance to endocrine therapy. Molibresib (GSK525762) is a small-molecule inhibitor of bromodomain and extraterminal (BET) family proteins (BRD2, BRD3, BRD4, and BRDT). Preclinical data suggested that the combination of molibresib with endocrine therapy might overcome endocrine resistance. This study aimed to investigate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy [objective response rate (ORR)] of molibresib combined with fulvestrant in women with HR+/HER2− mBC. Patients and Methods: In this phase I/II dose-escalation and dose-expansion study, patients received oral molibresib 60 or 80 mg once daily in combination with intramuscular fulvestrant. Patients enrolled had relapsed/refractory, advanced/metastatic HR+/HER2− breast cancer with disease progression on prior treatment with an aromatase inhibitor, with or without a cyclin-dependent kinase 4/6 inhibitor. Results: The study included 123 patients. The most common treatment-related adverse events (AE) were nausea (52%), dysgeusia (49%), and fatigue (45%). At a 60-mg dosage of molibresib, >90% of patients experienced treatment-related AE. Grade 3 or 4 treatment-related AE were observed in 47% and 48% of patients treated with molibresib 60 mg and molibresib 80 mg, respectively. The ORR was 13% [95% confidence interval (CI), 8–20], not meeting the 25% threshold for proceeding to phase II. Among 82 patients with detected circulating tumor DNA and clinical outcome at study enrollment, a strong association was observed between the detection of copy-number amplification and poor progression-free survival (HR, 2.89; 95% CI, 1.73–4.83; P < 0.0001). Conclusions: Molibresib in combination with fulvestrant did not demonstrate clinically meaningful activity in this study.

Year:

2023

Year:

2023

Year:

2023

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2022

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2022

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2022

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2022

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2021

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2021

Year:

2021

Year:

2021

Collaborators (11)

Elizabeth Chiao

Professor

The University of Texas MD Anderson Cancer Center

UNITED STATES
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Lee Ratner

Professor

Washington University School of Medicine

UNITED STATES
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Jinani Jayasekera

University of Michigan

UNITED STATES
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Ronald Mitsuyasu

Professor

University of California, Los Angeles

UNITED STATES
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Sunil Badve

Vice Chair/ Professor

Emory University

UNITED STATES
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Seema Khan

Professor

Northwestern University Feinberg School of Medicine

UNITED STATES
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Yaguang Wei

Assistant Professor

Icahn School of Medicine at Mount Sinai

UNITED STATES
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Antonio Wolff

Professor of Oncology

Johns Hopkins University

UNITED STATES
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Claudine Isaacs

Professor of Medicine

Georgetown University

UNITED STATES
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Timothy J Whelan

-

CANADA
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Missak Haigentz

Professor of Medicine and Chief, Thoracic and Head & Neck Medical Oncology

Rutgers Cancer Institute of New Jersey

UNITED STATES
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